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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 6 of 6 Results
Related Medical Device Recalls
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Product Description
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Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-2006-2021 - Verigene Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) Model Number: 20-006-024 2 07/02/2021 Luminex Corporation
Z-2007-2021 - Verigene Gram-Positive Blood Culture Nucleic Acid Test (BC-GP) Model Number: 20-006-018 2 07/02/2021 Luminex Corporation
Z-2011-2021 - Verigene Gram Negative Blood Culture Nucleic Acid Test v2 (BC-GNv2) Model Number: 20-006-026 2 07/02/2021 Luminex Corporation
Z-2009-2021 - Verigene Enteric Pathogens Nucleic Acid Test (EP) Model Number: 20-006-023 2 07/02/2021 Luminex Corporation
Z-2010-2021 - Verigene Clostridium difficile Nucleic Acid Test Kit (CDF) Model Number: 20-006-022 2 07/02/2021 Luminex Corporation
Z-2008-2021 - Verigene Gram Negative Blood Culture Nucleic Acid Test (BC-GN) Model Number: 20-006-021 2 07/02/2021 Luminex Corporation
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